scholarly journals XIII.—On the Application of Hamilton's Characteristic Function to Special Cases of Constraint

1865 ◽  
Vol 24 (1) ◽  
pp. 147-166 ◽  
Author(s):  
Tait
Keyword(s):  
Differential Equation ◽  
Partial Differential Equation ◽  
Characteristic Function ◽  
Complete Solution ◽  
Conservative System ◽  
First Order ◽  
Special Cases ◽  
General Method ◽  
Made In

One of the grandest steps which has ever been made in Dynamical Science is contained in two papers, “On a General Method in Dynamics” contributed to the Philosophical Transactions for 1834 and 1835 by Sir W. R. Hamilton. It is there shown that the complete solution of any kinetical problem, involving the action of a given conservative system of forces, and constraint depending upon the reaction of smooth guiding curves or surfaces, also given, is reducible to the determination of a single quantity called the Characteristic Function of the motion. This quantity is to be found from a partial differential equation of the first order, and second degree; and it has been shown that, from any complete integral of this equation, all the circumstances of the motion may be deduced by differentiation. So far as I can discover, this method has not been applied to inverse problems, of the nature of the Brachistochrone for instance, where the object aimed at is essentially the determination of the constraint requisite to produce a given result. It is easy to see, however, that a large class of such questions may be treated successfully by a process perfectly analogous to that of Hamilton; though the characteristic function in such cases is not the same function (of the quantities determining the motion) as that of the Method of Varying Action.

ESTIMATES FOR APPROXIMATE SOLUTIONS TO A FUNCTIONAL DIFFERENTIAL EQUATION MODEL OF CELL DIVISION

2021 ◽  
pp. 1-20
Author(s):  
STEPHEN TAYLOR ◽  
XUESHAN YANG
Keyword(s):  
Differential Equation ◽  
Partial Differential Equation ◽  
Cell Division ◽  
Nonnegative Function ◽  
Approximate Solutions ◽  
Equation Model ◽  
Order Partial Differential Equation ◽  
Partial Differential ◽  
First Order ◽  
Functional Differential

Abstract The functional partial differential equation (FPDE) for cell division, $$ \begin{align*} &\frac{\partial}{\partial t}n(x,t) +\frac{\partial}{\partial x}(g(x,t)n(x,t))\\ &\quad = -(b(x,t)+\mu(x,t))n(x,t)+b(\alpha x,t)\alpha n(\alpha x,t)+b(\beta x,t)\beta n(\beta x,t), \end{align*} $$ is not amenable to analytical solution techniques, despite being closely related to the first-order partial differential equation (PDE) $$ \begin{align*} \frac{\partial}{\partial t}n(x,t) +\frac{\partial}{\partial x}(g(x,t)n(x,t)) = -(b(x,t)+\mu(x,t))n(x,t)+F(x,t), \end{align*} $$ which, with known $F(x,t)$ , can be solved by the method of characteristics. The difficulty is due to the advanced functional terms $n(\alpha x,t)$ and $n(\beta x,t)$ , where $\beta \ge 2 \ge \alpha \ge 1$ , which arise because cells of size x are created when cells of size $\alpha x$ and $\beta x$ divide. The nonnegative function, $n(x,t)$ , denotes the density of cells at time t with respect to cell size x. The functions $g(x,t)$ , $b(x,t)$ and $\mu (x,t)$ are, respectively, the growth rate, splitting rate and death rate of cells of size x. The total number of cells, $\int _{0}^{\infty }n(x,t)\,dx$ , coincides with the $L^1$ norm of n. The goal of this paper is to find estimates in $L^1$ (and, with some restrictions, $L^p$ for $p>1$ ) for a sequence of approximate solutions to the FPDE that are generated by solving the first-order PDE. Our goal is to provide a framework for the analysis and computation of such FPDEs, and we give examples of such computations at the end of the paper.

scholarly journals Interpretation of Frenkel’s theory of sintering considering evolution of activated pores: II. Model and reliability

2015 ◽  
Vol 47 (1) ◽  
pp. 89-94
Author(s):  
C.L. Yu ◽  
D.P. Gao ◽  
S.M. Chai ◽  
Q. Liu ◽  
H. Shi ◽  
...  
Keyword(s):  
Differential Equation ◽  
Partial Differential Equation ◽  
Liquid Phase ◽  
Liquid Phase Sintering ◽  
Order Partial Differential Equation ◽  
Partial Differential ◽  
First Order ◽  
Sintering Time ◽  
Sintering Mechanism ◽  
Cordierite Glass

Frenkel's liquid-phase sintering mechanism has essential influence on the sintering of materials, however, by which only the initial 10% during isothermal sintering can be well explained. To overcome this shortage, Nikolic et al. introduced a mathematical model of shrinkage vs. sintering time concerning the activated volume evolution. This article compares the model established by Nikolic et al. with that of the Frenkel's liquid-phase sintering mechanism. The model is verified reliable via training the height and diameter data of cordierite glass by Giess et al. and the first-order partial differential equation. It is verified that the higher the temperature, the more quickly the value of the first-order partial differential equation with time and the relative initial effective activated volume to that in the final equibrium state increases to zero, and the more reliable the model is.

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